Abstract
Three different methods that use a single ruthenium catalyst to enable the facile formation of meta- and para-substituted alkenylarenes have now been developed. The reactions proceed through a tandem alkenylation/decarboxylation process and provide several advantages over alternative approaches.
Original language | English |
---|---|
Pages (from-to) | 1086-1088 |
Number of pages | 3 |
Journal | Nature Chemistry |
Volume | 8 |
Issue number | 12 |
DOIs | |
Publication status | Published - 22 Nov 2016 |